Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs755174338
rs755174338
ERCC2
0.020 GeneticVariation BEFREE With XRCC1-Arg280His variants, there was no association with SCCHN risk. 21945240

2012
dbSNP: rs755174338
rs755174338
ERCC2
0.020 GeneticVariation BEFREE Genetic variants ERCC2 Lys751Gln (rs13181), ERCC2 Asp312Asn (rs1799793), XRCC1 Arg194Trp (rs1799782); XRCC1 Gln399Arg (rs25487), XRCC1 Arg280His (rs25489) and XRCC3 Thr241Met (rs861539) were analyzed in a primary study group comprising 169 patients with histologically confirmed HNSCC and 463 healthy control subjects. 21419115

2011